POLYETHYLENE MEDULLARY PLUG - STIIHMER/— 510(k) K830949

Name: FDA 510(k) clearance K830949
Creator: U.S. Food and Drug Administration
Published: 1983-04-12

Substantially Equivalent

Allo Pro Corp.

FDA 510(k) clearance K830949 for POLYETHYLENE MEDULLARY PLUG - STIIHMER/, Substantially Equivalent on 1983-04-12. Applicant: Allo Pro Corp.. Device class: 2.

Clearance details

Applicant: Allo Pro Corp.
Product code: Code LZN
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 1983-03-24
Decision date: 1983-04-12
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Walker, MI, US

Download summary PDF View on FDA.gov ↗

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Data sourced from openFDA. This site is unofficial and independent of the FDA.